Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes, For Subcutaneous or Intravenous Use, Rx Only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505 U.S.A., Made in Italy, NDC: 67457-246-00 (syringe), 67457-246-01 (carton).
Reported: November 16, 2022 Initiated: October 7, 2022 #D-0058-2023
Product Description
Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes, For Subcutaneous or Intravenous Use, Rx Only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505 U.S.A., Made in Italy, NDC: 67457-246-00 (syringe), 67457-246-01 (carton).
Reason for Recall
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
Details
- Recalling Firm
- Viatris Inc
- Units Affected
- 22400 syringes
- Distribution
- Nationwide in the USA
- Location
- Canonsburg, PA
Frequently Asked Questions
What product was recalled? ▼
Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes, For Subcutaneous or Intravenous Use, Rx Only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505 U.S.A., Made in Italy, NDC: 67457-246-00 (syringe), 67457-246-01 (carton).. Recalled by Viatris Inc. Units affected: 22400 syringes.
Why was this product recalled? ▼
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 16, 2022. Severity: Critical. Recall number: D-0058-2023.
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